A Study Evaluating the Safety and Efficacy of the 3M™ V.A.C. Peel and Place Dressing
Trial Parameters
Brief Summary
The purpose of this clinical study is to obtain post-market safety and efficacy data when the V.A.C.® Peel and Place dressing is used in conjunction with 3M™ V.A.C.® Therapy.
Eligibility Criteria
Inclusion Criteria: 1. Subject is at least 22 years old at the time of consent. 2. Subject or legally authorized representative (LAR) is able to provide informed consent. 3. Subject has a wound deemed appropriate for treatment with a V.A.C.® Peel and Place dressing (used in conjunction with 3M™ V.A.C.® Therapy), according to the instructions for use for the dressing, including the following wound types: * an open wound: traumatic wound, dehisced surgical wound within 30 days of surgery, burn, venous ulcer, diabetic ulcer, or pressure ulcer Note: Prior to initial placement, the wound may be debrided, as clinically indicated * a closed or covered wound secured with sutures or staples: closed surgical incision, skin flap closure, or skin graft (recipient site) 4. Subject is willing and able to attend all study visits. Exclusion Criteria: 1. Subject is pregnant or lactating prior to application of the initial dressing. \* \*Women who have had surgical sterilization by a medically accepted